ClinVar Miner

Submissions for variant NM_001041.4(SI):c.1506T>G (p.Leu502=)

dbSNP: rs113511967
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522434 SCV001731979 benign not provided 2024-01-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501844 SCV002798046 likely benign Sucrase-isomaltase deficiency 2021-10-30 criteria provided, single submitter clinical testing

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